ACE2/ADAM17/TMPRSS2 interplay may be the main risk factor for COVID-19

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Chi tiết về thư mục
Tác giả chính: Zipeto, Donato
Ngày xuất bản: 2020
Tác giả khác: Palmeira, Julys da Fonseca, Argañaraz, Gustavo Adolfo, Argañaraz, Enrique Roberto
Định dạng: Article
Ngôn ngữ: eng
Nguồn: Repositório Institucional da UnB
Download full: https://repositorio.unb.br/handle/10482/39636
https://doi.org/10.3389/fimmu.2020.576745
Tóm tắt: The Coronavirus Disease 2019 (COVID-19) has already caused hundreds of thousands of deaths worldwide in a few months. Cardiovascular disease, hypertension, diabetes and chronic lung disease have been identified as the main COVID-19 comorbidities. Moreover, despite similar infection rates between men and women, the most severe course of the disease is higher in elderly and co-morbid male patients. Therefore, the occurrence of specific comorbidities associated with renin–angiotensin system (RAS) imbalance mediated by the interaction between angiotensin-converting enzyme 2 (ACE2) and desintegrin and metalloproteinase domain 17 (ADAM17), along with specific genetic factors mainly associated with type II transmembrane serine protease (TMPRSS2) expression, could be decisive for the clinical outcome of COVID-19. Indeed, the exacerbated ADAM17—mediated ACE2, TNF-α, and IL-6R secretion emerges as a possible underlying mechanism for the acute inflammatory immune response and the activation of the coagulation cascade. Therefore, in this review, we focus on the main pathophysiological aspects of ACE2, ADAM17, and TMPRSS2 host proteins in COVID-19. Additionally, we discuss a possible mechanism to explain the deleterious effect of ADAM17 and TMPRSS2 over-activation in the COVID-19 outcome.
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author Zipeto, Donato
author2 Palmeira, Julys da Fonseca
Argañaraz, Gustavo Adolfo
Argañaraz, Enrique Roberto
author2_role author
author
author
author_browse Argañaraz, Enrique Roberto
Argañaraz, Gustavo Adolfo
Palmeira, Julys da Fonseca
Zipeto, Donato
author_facet Zipeto, Donato
Palmeira, Julys da Fonseca
Argañaraz, Gustavo Adolfo
Argañaraz, Enrique Roberto
author_role author
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collection Repositório Institucional da UnB
dc.contributor.author.fl_str_mv Zipeto, Donato
Palmeira, Julys da Fonseca
Argañaraz, Gustavo Adolfo
Argañaraz, Enrique Roberto
dc.date.accessioned.fl_str_mv 2020-11-16T20:09:53Z
dc.date.available.fl_str_mv 2020-11-16T20:09:53Z
dc.date.issued.fl_str_mv 2020-10-07
dc.identifier.citation.fl_str_mv ZIPETO, Donato et al. ACE2/ADAM17/TMPRSS2 interplay may be the main risk factor for COVID-19. Frontiers in Immunology, v. 11, art. 576745, out. 2020. DOI: https://doi.org/10.3389/fimmu.2020.576745. Disponível em: https://www.frontiersin.org/articles/10.3389/fimmu.2020.576745/full. Acesso em: 16 nov. 2020.
dc.identifier.doi.pt_BR.fl_str_mv https://doi.org/10.3389/fimmu.2020.576745
dc.identifier.uri.fl_str_mv https://repositorio.unb.br/handle/10482/39636
dc.language.iso.fl_str_mv eng
dc.publisher.none.fl_str_mv Frontiers
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
dc.source.none.fl_str_mv reponame:Repositório Institucional da UnB
instname:Universidade de Brasília (UnB)
instacron:UNB
dc.subject.keyword.pt_BR.fl_str_mv ADAM17
ACE2
TMPRSS2
SARS-CoV-2
Covid-19
dc.title.pt_BR.fl_str_mv ACE2/ADAM17/TMPRSS2 interplay may be the main risk factor for COVID-19
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
description The Coronavirus Disease 2019 (COVID-19) has already caused hundreds of thousands of deaths worldwide in a few months. Cardiovascular disease, hypertension, diabetes and chronic lung disease have been identified as the main COVID-19 comorbidities. Moreover, despite similar infection rates between men and women, the most severe course of the disease is higher in elderly and co-morbid male patients. Therefore, the occurrence of specific comorbidities associated with renin–angiotensin system (RAS) imbalance mediated by the interaction between angiotensin-converting enzyme 2 (ACE2) and desintegrin and metalloproteinase domain 17 (ADAM17), along with specific genetic factors mainly associated with type II transmembrane serine protease (TMPRSS2) expression, could be decisive for the clinical outcome of COVID-19. Indeed, the exacerbated ADAM17—mediated ACE2, TNF-α, and IL-6R secretion emerges as a possible underlying mechanism for the acute inflammatory immune response and the activation of the coagulation cascade. Therefore, in this review, we focus on the main pathophysiological aspects of ACE2, ADAM17, and TMPRSS2 host proteins in COVID-19. Additionally, we discuss a possible mechanism to explain the deleterious effect of ADAM17 and TMPRSS2 over-activation in the COVID-19 outcome.
eu_rights_str_mv openAccess
format article
id UNB_801837840f00a4c1beb1fb95fda7c8b5
identifier_str_mv ZIPETO, Donato et al. ACE2/ADAM17/TMPRSS2 interplay may be the main risk factor for COVID-19. Frontiers in Immunology, v. 11, art. 576745, out. 2020. DOI: https://doi.org/10.3389/fimmu.2020.576745. Disponível em: https://www.frontiersin.org/articles/10.3389/fimmu.2020.576745/full. Acesso em: 16 nov. 2020.
instacron_str UNB
institution UNB
instname_str Universidade de Brasília (UnB)
language eng
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oai_identifier_str oai:repositorio.unb.br:10482/39636
publishDate 2020
publishDateSort 2020
publisher.none.fl_str_mv Frontiers
reponame_str Repositório Institucional da UnB
repository.mail.fl_str_mv repositorio@unb.br
repository.name.fl_str_mv Repositório Institucional da UnB - Universidade de Brasília (UnB)
repository_id_str
spelling Zipeto, DonatoPalmeira, Julys da FonsecaArgañaraz, Gustavo AdolfoArgañaraz, Enrique Roberto2020-11-16T20:09:53Z2020-11-16T20:09:53Z2020-10-07ZIPETO, Donato et al. ACE2/ADAM17/TMPRSS2 interplay may be the main risk factor for COVID-19. Frontiers in Immunology, v. 11, art. 576745, out. 2020. DOI: https://doi.org/10.3389/fimmu.2020.576745. Disponível em: https://www.frontiersin.org/articles/10.3389/fimmu.2020.576745/full. Acesso em: 16 nov. 2020.https://repositorio.unb.br/handle/10482/39636https://doi.org/10.3389/fimmu.2020.576745FrontiersCopyright © 2020 Zipeto, Palmeira, Argañaraz and Argañaraz. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.info:eu-repo/semantics/openAccessACE2/ADAM17/TMPRSS2 interplay may be the main risk factor for COVID-19info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleADAM17ACE2TMPRSS2SARS-CoV-2Covid-19The Coronavirus Disease 2019 (COVID-19) has already caused hundreds of thousands of deaths worldwide in a few months. Cardiovascular disease, hypertension, diabetes and chronic lung disease have been identified as the main COVID-19 comorbidities. Moreover, despite similar infection rates between men and women, the most severe course of the disease is higher in elderly and co-morbid male patients. Therefore, the occurrence of specific comorbidities associated with renin–angiotensin system (RAS) imbalance mediated by the interaction between angiotensin-converting enzyme 2 (ACE2) and desintegrin and metalloproteinase domain 17 (ADAM17), along with specific genetic factors mainly associated with type II transmembrane serine protease (TMPRSS2) expression, could be decisive for the clinical outcome of COVID-19. Indeed, the exacerbated ADAM17—mediated ACE2, TNF-α, and IL-6R secretion emerges as a possible underlying mechanism for the acute inflammatory immune response and the activation of the coagulation cascade. Therefore, in this review, we focus on the main pathophysiological aspects of ACE2, ADAM17, and TMPRSS2 host proteins in COVID-19. Additionally, we discuss a possible mechanism to explain the deleterious effect of ADAM17 and TMPRSS2 over-activation in the COVID-19 outcome.engreponame:Repositório Institucional da UnBinstname:Universidade de Brasília (UnB)instacron:UNBORIGINALARTIGO_ACE2ADAM17TMPRSS2Interplay.pdfARTIGO_ACE2ADAM17TMPRSS2Interplay.pdfapplication/pdf766389http://repositorio2.unb.br/jspui/bitstream/10482/39636/1/ARTIGO_ACE2ADAM17TMPRSS2Interplay.pdf7da6b803334a77476620914b0d321201MD51open accessLICENSElicense.txtlicense.txttext/plain163http://repositorio2.unb.br/jspui/bitstream/10482/39636/2/license.txtba54f8d1c5f5ec8df897ad678916c701MD52open access10482/396362023-05-23 21:10:22.148open accessoai:repositorio.unb.br:10482/39636U3VibWlzc8OjbyBlZmV0aXZhZGEgcG9yIGludGVncmFudGUgZGEgZXF1aXBlIGRvIFJlcG9zaXTDs3JpbyBJbnN0aXR1Y2lvbmFsIGRhIFVuQiBkZSBhY29yZG8gY29tIGxpY2Vuw6dhIGNvbmNlZGlkYSBwZWxvIGF1dG9yIGUvb3UgZGV0ZW50b3IgZG9zIGRpcmVpdG9zIGF1dG9yYWlzLg==Repositório InstitucionalPUBhttps://repositorio.unb.br/oai/requestrepositorio@unb.bropendoar:2023-05-24T00:10:22Repositório Institucional da UnB - Universidade de Brasília (UnB)
spellingShingle ACE2/ADAM17/TMPRSS2 interplay may be the main risk factor for COVID-19
Zipeto, Donato
ADAM17
ACE2
TMPRSS2
SARS-CoV-2
Covid-19
status_str publishedVersion
title ACE2/ADAM17/TMPRSS2 interplay may be the main risk factor for COVID-19
title_full ACE2/ADAM17/TMPRSS2 interplay may be the main risk factor for COVID-19
title_fullStr ACE2/ADAM17/TMPRSS2 interplay may be the main risk factor for COVID-19
title_full_unstemmed ACE2/ADAM17/TMPRSS2 interplay may be the main risk factor for COVID-19
title_short ACE2/ADAM17/TMPRSS2 interplay may be the main risk factor for COVID-19
title_sort ACE2/ADAM17/TMPRSS2 interplay may be the main risk factor for COVID-19
topic ADAM17
ACE2
TMPRSS2
SARS-CoV-2
Covid-19
url https://repositorio.unb.br/handle/10482/39636
https://doi.org/10.3389/fimmu.2020.576745